about
Solution structure of chicken liver basic fatty acid binding proteinSolution structure of the beta-subunit of the translation initiation factor aIF2 from archaebacteria Sulfolobus solfataricusComprehensive analysis of blood group antigen binding to classical and El Tor cholera toxin B-pentamers by NMR.Insights into the Binding of Cyclic RGD Peptidomimetics to α5β1 Integrin by using Live-Cell NMR And Computational Studies.Insight to the binding mode of triazole RGD-peptidomimetics to integrin-rich cancer cells by NMR and molecular modeling.Determination of the binding epitope of RGD-peptidomimetics to αvβ3 and α(IIb)β3 integrin-rich intact cells by NMR and computational studies.Dimeric Smac mimetics/IAP inhibitors as in vivo-active pro-apoptotic agents. Part II: Structural and biological characterization.Design, synthesis, and biological evaluation of novel cRGD-paclitaxel conjugates for integrin-assisted drug delivery.STD and trNOESY NMR study of receptor-ligand interactions in living cancer cells.Rational design, synthesis and characterization of potent, non-peptidic Smac mimics/XIAP inhibitors as proapoptotic agents for cancer therapy.Sequence specific peptidomimetic molecules inhibitors of a protein-protein interaction at the helix 1 level of c-Myc.Antitumor activity of a novel homodimeric SMAC mimetic in ovarian carcinoma.Both El Tor and classical cholera toxin bind blood group determinants.Synthesis of novel DC-SIGN ligands with an alpha-fucosylamide anchor.A NMR and computational study of Smac mimics targeting both the BIR2 and BIR3 domains in XIAP protein.A folding inhibitor of the HIV-1 protease.Identification of the folding inhibitors of hen-egg lysozyme: gathering the right tools.A Combined NMR-Computational Study of the Interaction between Influenza Virus Hemagglutinin and Sialic Derivatives from Human and Avian Receptors on the Surface of Transfected Cells.Homo- and heterodimeric Smac mimetics/IAP inhibitors as in vivo-active pro-apoptotic agents. Part I: SynthesisCyclic RGD Peptidomimetics Containing Bifunctional Diketopiperazine Scaffolds as New Potent Integrin LigandsExploration of ligand binding modes towards the identification of compounds targeting HuR: a combined STD-NMR and Molecular Modelling approachIdentification and characterization of folding inhibitors of hen egg lysozyme: An example of a new paradigm of drug designAnti-Multiple Myeloma Potential of Secondary Metabolites from Hibiscus sabdariffaExploring E-cadherin-peptidomimetics interaction using NMR and computational studies
P50
Q27640765-957B8AC4-5B23-44BD-ABBC-D84E70E5048BQ27649053-3EE612AD-7801-4E22-A408-1B79E161FEDDQ30820833-8EC50C1A-4A9C-4534-A51C-6A8514222EA4Q36272448-B21CD79E-5B7B-4561-A6C9-FCC4EE5FB38CQ38799015-0B17067C-B490-451E-9E68-BD7EE977022AQ39154695-F0D25555-936D-4D13-84FC-32DBD582364BQ39260309-22C271DE-1696-4803-9D60-FAB8DE69F7D1Q39318537-10865E91-3AC0-4F75-8620-6368F345150FQ39576029-D0E63504-66F9-4941-BB32-0D844B353BE5Q39822939-464F7653-AB19-44CA-AE14-19E03280AAABQ40465567-BDE7733B-F93B-4934-9EFC-091A3800E6F3Q44134106-D8AD8393-D36A-4430-B761-69B35BB46CC5Q44408071-94154DA2-0C5B-4A14-9A1B-AE01F7D754A5Q46462857-963D2A5F-0D13-4610-A891-9ECD8CC643EDQ46806247-81466523-2F78-4013-8EE3-F58083C4CCA0Q46873034-C6A416F7-22CA-48F4-97B0-587388274977Q51748563-4AD815E7-9CA4-4D25-96F7-6818BCCB15C9Q52309710-1CEE1B80-5012-48ED-99DF-FD198C7F6665Q56877461-20D8A493-6319-42CB-A9E8-7B65C73AF0E8Q57973207-F36934F0-DBB7-4890-8EE0-7EFF1D6B7222Q58743732-CFF2FF22-7CF8-49BA-BEAF-663B199411E7Q58882307-F36BF12B-AB06-4735-AB36-D7704D03F168Q92027559-91B53030-7063-4692-AA51-6C3F42ADAE7CQ92488134-8919B98E-7194-4F27-BBA2-4A8FFE7ACA6C
P50
description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Francesca Vasile
@ast
Francesca Vasile
@en
Francesca Vasile
@es
Francesca Vasile
@nl
type
label
Francesca Vasile
@ast
Francesca Vasile
@en
Francesca Vasile
@es
Francesca Vasile
@nl
prefLabel
Francesca Vasile
@ast
Francesca Vasile
@en
Francesca Vasile
@es
Francesca Vasile
@nl
P106
P1153
6602849908
P31
P496
0000-0002-3926-8261